Candesartan Cilexetil EP impurity B
Synonyms: Candesartan Cilexetil - Impurity B · Desethyl Candesartan Cilexetil
Candesartan Cilexetil EP impurity B (CAS 869631-11-8) – Candesartan impurity standard. C31H30N6O6, MW 582.6. Vaqora Chemicals: COA, global shipping.
About Candesartan Cilexetil EP impurity B
Vaqora Chemicals supplies Candesartan Cilexetil EP impurity B, a pharmacopeial impurity of Candesartan registered under CAS number 869631-11-8. The compound has the formula C31H30N6O6, corresponding to a molecular weight of 582.6 g/mol. Alternative names: Candesartan Cilexetil - Impurity B and Desethyl Candesartan Cilexetil.
The product is provided as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. Handle it with standard laboratory precautions and appropriate personal protective equipment.
This Candesartan impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF filings. Our customers for this product work in pharmaceutical manufacturing and academic and industrial research.
Vaqora Chemicals supplies Candesartan Cilexetil EP impurity B in 10 mg, 25 mg, 50 mg and 100 mg packs, each shipped with a Certificate of Analysis (COA), and exports worldwide.
Typical applications
- Pharmacopeial method verification
- Impurity profiling
- QC release testing
- ANDA / DMF filings
Industries
View every impurity, metabolite and intermediate we list for Candesartan.
Candesartan impuritiesGrade guides
Specifications & identifiers
| Product name | Candesartan Cilexetil EP impurity B |
|---|---|
| Catalogue No. | VQ-021971 |
| CAS Number | 869631-11-8 |
| IUPAC name | 1-cyclohexyloxycarbonyloxyethyl 2-oxo-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]-1H-benzimidazole-4-carboxylate |
| Molecular formula | C31H30N6O6 |
| Molecular weight | 582.6 g/mol |
| Exact mass | 582.2227 |
| Grade | Reference Standard |
| HSN code | 38229090 |
| InChIKey | UEJMFQHOVKQHHB-UHFFFAOYSA-N |
| SMILES | CC(OC(=O)C1=C2C(=CC=C1)NC(=O)N2CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)OC(=O)OC6CCCCC6 |
| PubChem CID | 46783540 |
| Physical form | Solid |
|---|---|
| LogP (XLogP3) | 5.6 |
| H-bond donors / acceptors | 2 / 9 |
| TPSA | 149 Ų |
Documents
Frequently asked questions
What is the CAS number of Candesartan Cilexetil EP impurity B?
The CAS Registry Number of Candesartan Cilexetil EP impurity B is 869631-11-8. It is also known as Candesartan Cilexetil - Impurity B, Desethyl Candesartan Cilexetil.
What is the molecular formula and molecular weight of Candesartan Cilexetil EP impurity B?
Candesartan Cilexetil EP impurity B has the molecular formula C31H30N6O6 and a molecular weight of 582.6 g/mol. Its IUPAC name is 1-cyclohexyloxycarbonyloxyethyl 2-oxo-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]-1H-benzimidazole-4-carboxylate.
What is Candesartan Cilexetil EP impurity B used for?
Candesartan Cilexetil EP impurity B is supplied as a characterised reference material related to Candesartan. It is used for analytical method development and validation (AMV), impurity profiling, stability studies and quality control, and in ANDA/DMF regulatory filings.
Which grade and pack sizes of Candesartan Cilexetil EP impurity B can I order?
We supply Candesartan Cilexetil EP impurity B in Reference Standard grade, in 10 mg, 25 mg, 50 mg, 100 mg packs. Larger bulk quantities and custom packing are quoted on request.
Do you provide a COA and SDS with Candesartan Cilexetil EP impurity B?
Yes. Every lot of Candesartan Cilexetil EP impurity B is shipped with a batch-specific Certificate of Analysis, and a 16-section GHS Safety Data Sheet is provided with the quotation and the shipment.
Can Candesartan Cilexetil EP impurity B be shipped internationally?
Yes. We export Candesartan Cilexetil EP impurity B worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.
Enquire about Candesartan Cilexetil EP impurity B
We reply within one business day with price, pack options, lead time and documentation.
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